F-0195-2016 Class II Terminated

Recalled by S. Martinelli & Co — Watsonville, CA

FDA food recall F-0195-2016 was initiated by S. Martinelli & Co on Oct 15, 2015 and is designated Class II. Reason for recall: Potential for glass fragments in 8.4 oz. bottles of four varieties of sparkling cider. The recall status is terminated (terminated May 1, 2017). Affected quantity: 166,804 trays of 12 packs, 31,939 trays of 4-6 packs.

Recall Details

Product Type
Food
Report Date
Nov 25, 2015
Initiation Date
Oct 15, 2015
Termination Date
May 1, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
166,804 trays of 12 packs, 31,939 trays of 4-6 packs

Product Description

Martinelli's Gold Medal Sparkling Cider, 8.4 oz glass bottles; Packed in 12 pack, UPC 0 41244 00256; item number 12256; 4/6 packs, Tray UPC 0 41244-99932 3, item number 46256; 6 pack Retail UPC 0 41244 46256 8. Single 8.4 oz. bottle, UPC 041244 00256 6

Reason for Recall

Potential for glass fragments in 8.4 oz. bottles of four varieties of sparkling cider.

Distribution Pattern

US and Japan, Virgin Islands, India, Costa Rica, Honduras, El Salvador, Nicaragua, Guatemala, Panama, Aruba, Jamaica, Barbados, Trinidad/Tobago, Dominican Republic, US Virgin Islands, Columbia, American Samoa, Curacao, Guam, Grand Cayman Islands, St. Croix, St. Marten, St. Thomas and Fiji. Shipments to Costco in Japan, and to India and Fiji, were made to a distributor, Otis McAllister, Inc., 300 Frank H. Ogawa Plaza, suite 400, Oakland, CA 94612, which then sold the product to the retailer in those countries.

Code Information

12 pack:Best Before dates include 03/05/2018 to 04/11/2018. 6 pack Best Befroe dates include 3/02/2018 to 04/15/2018.

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0195-2016
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for F-0195-2016. Report a data issue: hello@regdatalab.com.